MeSH Treeview
Query OMIM entry list
608217
EBN3
EPILEPSY, BENIGN NEONATAL, 3
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High-scoring List
Genetic Phenomena
Genetic Processes
DNA Damage
DNA Breaks
Chromosome Breakage
Mutagenesis
Sequence Inversion
Chromosome Inversion
Genetic Structures
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 4-5
Chromosomes, Human, Pair 5
Genetic Variation
Mutation
Chromosome Aberrations
Chromosome Breakage
Chromosome Inversion
Sequence Inversion
Chromosome Inversion
Database Center for Life Science
